HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84031838G>T , CM000678.2:g.84031838G>T | GRCh38 |
NC_000016.9:g.84065443G>T , CM000678.1:g.84065443G>T | GRCh37 |
NC_000016.8:g.82622944G>T | NCBI36 |
NG_034136.1:g.15320C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299709.8:c.632+29C>A MANE Select | ENSP00000299709.3:n.632+29C>A | |
ENST00000299709.7:c.632+29C>A | ENSP00000299709.3:n.632+29C>A | |
ENST00000568178.1:c.632+29C>A | ENSP00000457737.1:n.632+29C>A | |
NM_001080442.2:c.632+29C>A | NP_001073911.1:n.632+29C>A | |
XM_011522872.1:c.632+29C>A | XP_011521174.1:n.632+29C>A | |
XM_017022946.1:c.632+29C>A | XP_016878435.1:n.632+29C>A | |
NM_001080442.3:c.632+29C>A MANE Select | NP_001073911.1:n.632+29C>A |